NDC 0002-4112

Zyprexa

Olanzapine

Zyprexa is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is Olanzapine.

Product ID0002-4112_7184cd07-6f72-4413-9d11-daa74ef14b03
NDC0002-4112
Product TypeHuman Prescription Drug
Proprietary NameZyprexa
Generic NameOlanzapine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1997-06-23
Marketing CategoryNDA / NDA
Application NumberNDA020592
Labeler NameEli Lilly and Company
Substance NameOLANZAPINE
Active Ingredient Strength3 mg/1
Pharm ClassesAtypical Antipsychotic [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0002-4112-30

30 TABLET in 1 BOTTLE (0002-4112-30)
Marketing Start Date1997-06-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0002-4112-33 [00002411233]

Zyprexa TABLET
Marketing CategoryNDA
Application NumberNDA020592
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-06-23
Marketing End Date2013-08-06

NDC 0002-4112-07 [00002411207]

Zyprexa TABLET
Marketing CategoryNDA
Application NumberNDA020592
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-06-23
Marketing End Date2013-08-06

NDC 0002-4112-01 [00002411201]

Zyprexa TABLET
Marketing CategoryNDA
Application NumberNDA020592
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-06-23
Marketing End Date2013-08-06

NDC 0002-4112-04 [00002411204]

Zyprexa TABLET
Marketing CategoryNDA
Application NumberNDA020592
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-06-23
Marketing End Date2013-08-06

NDC 0002-4112-30 [00002411230]

Zyprexa TABLET
Marketing CategoryNDA
Application NumberNDA020592
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-06-23

Drug Details

Active Ingredients

IngredientStrength
OLANZAPINE2.5 mg/1

OpenFDA Data

SPL SET ID:d5051fbc-846b-4946-82df-341fb1216341
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 200034
  • 212405
  • 351108
  • 283639
  • 485968
  • 351107
  • 754506
  • 754505
  • 754504
  • 754503
  • 284514
  • 312077
  • 312076
  • 312079
  • 312078
  • 545353
  • 261337
  • 314154
  • 314155
  • 153047
  • 153046
  • 153048
  • UPC Code
  • 0300024420304
  • 0300024117303
  • 0300024415300
  • 0300024112308
  • 0300024115309
  • 0300024116306
  • Pharmacological Class

    • Atypical Antipsychotic [EPC]

    NDC Crossover Matching brand name "Zyprexa" or generic name "Olanzapine"

    NDCBrand NameGeneric Name
    0002-4112ZyprexaOlanzapine
    0002-4115ZyprexaOlanzapine
    0002-4116ZyprexaOlanzapine
    0002-4117ZyprexaOlanzapine
    0002-4415ZyprexaOlanzapine
    0002-4420ZyprexaOlanzapine
    0002-4453ZYPREXAOlanzapine
    0002-4454ZYPREXAOlanzapine
    0002-4455ZYPREXAOlanzapine
    68258-7092ZyprexaZyprexa
    68258-7093ZyprexaZyprexa
    68258-7090ZyprexaZyprexa
    68258-7091ZyprexaZyprexa
    70518-1465ZyprexaZyprexa
    21695-144ZyprexaZyprexa
    21695-140ZyprexaZyprexa
    21695-142ZyprexaZyprexa
    49999-606ZyprexaZyprexa
    52959-579ZyprexaZyprexa
    55289-213ZyprexaZyprexa

    Trademark Results [Zyprexa]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ZYPREXA
    ZYPREXA
    75078626 2072867 Live/Registered
    Eli Lilly and Company
    1996-03-26

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